Director, Cell Therapy Quality Automation

Bristol Myers Squibb

Devens, MA, US
Base: $188,250 - $250,929; bonus/equity: + incenti...
Hybrid (50% onsite)
Cell therapy quality processes
Next-generation quality systems
Automated processing integration
Bristol Myers Squibb is seeking a Director of Cell Therapy Quality Automation to oversee and implement advanced quality processes in high-volume manufacturing environments. The role requires extensive experience in quality systems and collaboration with cross-functional teams to enhance overall quality and compliance

Job Summary

  • This global position is responsible for the planning, execution, and implementation of next-generation quality processes to support high volume manufacturing processes.
  • The Director will be a core member of critical cross-functional teams which identifies the future state cell therapy value stream in conjunction with automated processing.
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Director of Cell Therapy Quality Automation to oversee and implement advanced quality processes in high-volume manufacturing environments. The role requires extensive experience in quality systems and collaboration with cross-functional teams to enhance overall quality and compliance.

Salary

Base: $188,250 - $250,929; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • Cell Therapy Quality Processes
  • Next-generation Quality Systems
  • Automated Processing Integration
  • Advanced Technologies Implementation
  • Industry Best Practices Adoption

Nice-to-have

  • Culture of Innovation
  • Continuous Improvement Mindset
  • Strategic Thinking Capability
  • Cross-functional Collaboration

Key Requirements

  • 14+ years of experience
  • Bachelor's degree in Engineering or Life Sciences
  • Strong knowledge of quality systems and regulatory requirements

Work Rights

Not specified

Tailored Resume

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